Synthetic cephalosporins

ABSTRACT

7-( Alpha -3-Acylureidophenylacetamido)- and 7-( Alpha -3acylureidothienylacetamido)cephalosporanic acids and the corresponding betaines and desacetoxy derivatives are valuable as antibacterial agents, as nutritional supplements in animal feeds and as therapeutic agents in poultry and animals, including man, and are especially useful in the treatment of infectious diseases caused by Gram-positive and Gram-negative bacteria, most particularly those caused by the Pseudomonas genus. 7-(D- Alpha (3-(2&#39;&#39;-furoyl)ureido)phenylacetamido)cephalosporanic acid, a preferred embodiment of the invention, is prepared by the treatment of 7-(D- Alpha -amino-phenylacetamido)cephalosporanic acid with 2-furoyl isocyanate.

United States Patent Holdrege 51 *Aug. 29, 1972 [54] SYNTHETIC CEPHALOSPORINS [21] Appl. No.: 792,757

[52] US. Cl. ..260/243 C, 424/246 [51] Int. Cl. ..C07d 99/24 [58] Field of Search ..260/243 C [56] References Cited UNITED STATES PATENTS 3,479,339 11/1969 Holdredge ..260/239.l 3,497,504 2/1970 Wagner ..260/239.1

Primary Examiner-Nicholas S. Rizzo Attorney-Herbert W. Taylor, Jr., Robert E. Havranek, Richard H. Brink and James Magee, Jr.

[57] ABSTRACT 7-(a-3-Acylureidophenylacetamido)- and 7-(a-3- acylureidothienylacetamido)cephalosporanic acids and the corresponding betaines and desacetoxy derivatives are valuable as antibacterial agents, as nutritional supplements in animal feeds and as therapeutic agents in poultry and animals, including man, and are especially useful in the treatment of infectious diseases caused by Gram-positive and Gramnegative bacteria, most particularly those caused by the Pseudomonas genus. 7- D-a-[3-(2'-furoyl)ureido]phenylacetamido cephalosporanic acid, a preferred embodiment of the invention, is prepared by the treatment of 7-(D-a-amino-phenylacetamido)cephalosporanic acid with Z-furoyl isocyanate.

19 Claims, No Drawings SYNTHETIC CEPHALOSPORINS BACKGROUND OF THE INVENTION 1. Field of the Invention.

The cephalosporins of the present invention possess the usual attributes of such compounds and are particularly useful in the treatment of Pseudomonas infections.

2. Description of the Prior Art.

Cephalothin and cephaloridine are well-known antibacterial agents. The literature also contains considerable data on the activity of cephaloglycin and cephalexin. The literature on cephalosporins has been reviewed by E. P. Abraham, Quart. Rev.(London), 21, 231 (1967), by E. Van I-Ieyninger, Advan. Drug Res., 4, 1-70, (1967) and briefly by L. C. Cheney, Annual Reports in Medicinal Chemistry, 1967, Academic Press lnc., 111 Fifth Avenue, New York, N.Y., 10003, on pages 96 and 97.

The preparation of various 7-[a-aminoarylacetamido]-cephalosporanic acids and the corresponding desacetoxy compounds in which arylrepresents unsubstituted or substituted phenyl or 2- or 3-thienyl is described in British Specifications 985,747, 1,017,624, 1,054,806 and 1,123,333, in Belgian Pat. No. 696,026 (Farmdoc No. 29,494), in U. S. Pat. Nos. 3,311,621 and 3,352,858, in Japanese Pat. No. 16871/66 (Farmdoc No. 23,231 by Spencer et al., J. Med. Chem., 9 (5), 746-750 (1966) and by Kurita et al. J. Antibiotics (Tokyo) (A) 19, 243249 (1966).

SUMMARY OF THE INVENTION This invention comprises antibacterial agents of the formula wherein Ar is Z-thienyl, 3-thienyl or in which each of R and R is hydrogen, nitro, di(lower)-alkylamino, (lower)alkanoylamino, amino, hydroxy, (lower)-alkanoyloxy, (lower)alkyl (comprising straight and branched chain saturated aliphatic groups having from one to six carbon atoms inclusive), (lower)alkoxy, sulfamyl, chloro, iodo, bromo, fluoro or trifluoromethyl;

A is hydrogen, acetoxy, pyridinium, picolinium or lutidinium;

M is hydrogen, a pharmaceutically acceptable, nontoxic cation or an anionic charge when A is one of said quaternary ammonium radicals; and

Z is (lower)all yl, cycloalkyl having four, five, six or seven carbon atoms, monohalo(lower)alkyl, dichloromethyl, trichloromethyl, (lower)a1kenyl of two to six carbon atoms,

n is an integer from 0 to 3 inclusive and each of R and R is hydrogen, nitro, di(lower)-alkylamino, (lower)alkanoylamino, (lower)alkanoyloxy, (lower)-alkyl (comprising straight and branched chain saturated aliphatic groups having from one to six carbon atoms inclusive), (lower)-a1koxy, sulfamyl, chloro, iodo, bromo, fluoro or trifluoromethyl.

Typical nontoxic, pharmaceutically acceptable metallic cations include sodium, potassium, calcium, aluminum, and the like, the ammonium cation and substituted ammonium cations, e.g., cations of such nontoxic amines as tri(lower)-alkylamines, i.e., triethylamine, etc., procaine, dibenzylamine, N-benzylbeta-phenethylamine, l-ephenamine, N,N'- dibenzylethylenediamine, dehydroabietylamine, N,N'- bis-dehydroabietylethylenediamine, N-(lower)alkylpiperidine, e.g., N-ethylpiperidine, or other such amines which have been used to form pharmaceutically acceptable nontoxic salts with benzylpenicillin. Where A is hydrogen or acetoxy these compounds preferably are prepared by treatment of the corresponding 11- amino compound with an acyl isocyanate.

In the preferred embodiment of the present invention, Ar is phenyl or thienyl, A is hydrogen, acetoxy or pyridinium and M and Z are as defined above. Within that group it is preferred that Z be one of the specified aromatic radicals and most preferably that Z be phenyl, 2- or 3-thienyl, 2-furyl or 5-nitr0-2-furyl and that the acarbon of the cephalosporin side chain (to which the acylureido group is attached)be of the D configuration.

DETAILED DESCRIPTION Antibacterial agents such as ampicillin and cephalothin have proved highly effective in the past in the therapy of infections due to Gram-positive and Gram-negative bacteria but these compounds have been notably lacking in their ability to effectively control Pseudomonas infection. Carbenicillin is active against Pseudomonas only in high concentrations and is useful in such infections in man only when give by injection. 7

It was an object of the present invention to provide compounds useful in the treatment of infections casued by Gram-positive and Gram-negative bacteria, including particularly those caused by Pseudomonas aeruginosa.

The compounds of the present invention as defined above under Summary of the Invention are particularly useful in that they possess antibacterial activity against both Gram-positive and Gram-negative bacteria, and most particularly exhibit activity against 5 Pseudomonas aeruginosa infections.

The a-carbon atom of the cephalosporin side chain (to which the acylureido group is attached) is an asymmetric carbon atom and the compounds of this invention can therefore exist in two optically active isomeric forms [the D- and L- diastereoisomers], as well as in the DL form which is a mixture of the two optically active forms; all such isomeric forms of the compounds are included within the scope of the present invention but the D form is preferred. Also included within the scope of the present invention are easily hydrolyzed esters which are converted to the free acid form by chemical or enzymatic hydrolysis including those of the type described in U. 8 Pat. No. 3,284,451.

It should be noted in connection with the foregoing consideration of the diastereoisomers of this invention that isomers other than the two caused by the asymmetric carbon of the side chain are possible due to the presence of asymmetric carbon atoms in the 7- aminocephalosporanic acid nucleus. Such additional isomers, however, are not presently significant since 7- aminocephalosporanic acid which is the product of fermentation processes is consistently of one configuration; such 7-aminocephalosporanic acid is presently used in the production of the compounds of this invention.

One method for the preparation of certain of the compounds of the present invention comprises wherein A is hydrogen or acetoxy and Ar is as defined above or a monohydrate or polyhydrate or salt thereof,

with an acyl isocyanate having the formula wherein Z is (lower)alkyl, cycloalkyl having four, five,

six or seven carbon atoms, monohalo(lower)alkyl, dichloromethyl, trichloromethyl, (lower)alkenyl of two to six carbon atoms,

wherein n is an integer from 0 to 3 inclusive and each of R and R is hydrogen, nitro, di(lower)alkylamino, (lower)alkanoylamino, (lower)alkanoyloxy, (lower)alkyl (comprising straight and branched chain saturated aliphatic groups having from one .to six carbon atoms inclusive), (lower)alkoxy, sulfamyl, chloro, iodo, bromo, fluoro or trifluoromethyl, preferably in a ratio of 1.0 to 1.5 equivalents of the acyl isocyanate per equivalent of the cephalosporin acid in the presence of a base, preferably an organic base such as N-methylpiperidine, tri(lower)alkylamine, or the like, but preferably in the presence of triethylamine preferably in a ratio of one to two moles of amine per mole of the cephalosporin acid. in an anhydrous inert solvent such as dimethylformamide, dimethylsulfoxide, chloroform, tetrahydrofuran, n-pentane, methylene chloride, but preferably methylene chloride, at a temperature in the range of about 20 to 50 C., but preferably about 0 to 20 C for a periof of time of at least 30 minutes, with agitation to produce a compound having the formula wherein A is hydrogen or acetoxy and Ar and Z are as defined above, or a salt thereof. The betaines are produced by reaction the compounds above in which A is acetoxy with pyridine, picoline or lutidine by the method of Spencer et al., J. Org. Chem 32, 500 (1967).

Another method for the preparation of the compounds of the present invention comprises reacting a compound of the formula wherein A and M are as defined above (preferably in the form of a neutral salt such as the sodium salt or the triethylamine salt) with an acid having the formula (wherein Ar and Z are as defined above) or with its functional equivalent as an acylating agent for a primary amino group. The preferred reagent is the mixed anhydride prepared by reacting such an acid with isovaleryl chloride (or pivaloyl chloride) in the presence of a tertiary amine such as triethylamine as an acceptor of hydrogen chloride. Such equivalents include the corresponding carboxylic chlorides, bromides, acid anhydrides, including mixed anhydrides and particularly the mixed anhydrides prepared from stronger acids such as the lower aliphatic monoesters of carbonic acid, of alkyl and aryl sulfonic acids and of more hindered acids such as diphenylacetic acid and isovaleric acid. In addition, an acid azide or an active ester or thioester (e.g., with p-nitrophenol, 2,4- dinitrophenol, thiophenol, thioacetic acid) may be used or the free acid itself may be coupled with 7- aminocephalosporanic acid after first reacting said free acid with N,N-dimethylchloroformiminium chloride [cf. Great Britain 1,008,170 and Novak and Weichet, Experientia XXI/6, 360 (1965)] or by the use of enzymes or of an N,N-carbonyldiimidazole or an N,N'- carbonylditriazole [cf. South African Patent Specification 63/2684] of a carbodiimide reagent [especially N,N'-dicyclohexylcarbodiimide, N,N-diisopropylcarbodiimide or N-cyclohexyl-N'-(2-morpholinoethyl) carbodiimide; cf. Sheehan and Hess, J. Amer. Chem. Soc. 77, 1067, (1955) or of alkynylamine reagent [cf. R. Buijle and H. G. Viehe, Angew. Chem. International Edition 3, 582 (1964)], or of a ketenimine reagent [cf. C. L. Stevens and M. E. Monk, J. Amer. Chem. Soc. 80, 4065 (1958)] or of an isoxazolium salt reagent [cf. R. B. Woodword, R. A. Olofson and 1-1. Mayer, J. Amer. Chem. Soc. 83, 1010 (1961 )1. Another equivalent of the acid chloride is a corresponding azolide, i.e., an amide of the corresponding acid whose amide nitrogen is a member of a quasiaromat'ic fivemembered ring containing at least two nitrogen atoms, i.e., imidazole, pyrazole, the triazoles, benzimidazole, benzotriazole and their substituted derivatives. As an example of the general method for the preparation of an azolide, N-,N'-carbonyldiimidazole is reacted with a carboxylic acid in equimolar proportions at room temperature in tetrahydrofuran, chloroform, dimethylformamide or a similar inert solvent to form the carboxylic acid imidazolide in practically quantitative yield with liberation of carbon dioxide and one mole of imidazole. Dicarboxylic acids yield diimidazolides. The byproduct, imidazole, precipitates and may be separated and the imidazolide isolated, but this is not essential. The methods for carrying out these reactions to produce a cephalosporin and the methods used to isolate the cephalosporin so-produced are well-known in the art (cf. U. S. Pats. Nos. 3,079,314, 3,117,126 and 3,129,224 and British Pats. Nos. 932,644, 957,570, and 959,054).

The compounds used in the present invention include 7-aminocephalosporanic acid and derivatives thereof. 7-Aminocephalosporanic acid is prepared by hydrolysis of cephalosporin C and has the formula l coon Treatment of cephalosporin C with a tertiary amine, e.g., pyridine, lutidines, picolines and the like, followed by acid hydrolysis produces a nucleus which, in the case of pyridine, has the formula and has been given the name 3-pyridiniummethyl-7- aminodecephalosporanic acid inner salt.

The foregoing muclei and the preparation thereof are known in the art and are described for example in U. S. Pat. No. 3,1 17,126 and British Pat. Nos. 932,644 957,570 and 959,054.

3-Methyl-7-aminodecephalosporanic acid having the is produced by catalytic reduction of cephalosporin C followed by hydrolytic removal of the S-aminoadipoyl side chain as described in U. S. Pat. No. 3,129,224.

The starting acids used above are prepared by replacing the cephalosporanic acid of the previous process with the simple amino acid of the formula in the reaction with the acyl isocyanate of the formula The 7-[aamino-arylacetamido]cephalosporanic acids and the corresponding desacetoxy compounds used above as starting materials are prepared from the corresponding a-azido-arylacetic acids and a-aminoarylacetic acids by the methods set out in the literature and particularly in the publications and patents listed above under the heading Description of the Prior Art. Many other oz-azidoand a-amino-arylacetic acids are described, for example, in U. S. Pat. Nos. 2,985,648, 3,140,282, 3,308,023, 3,316,247, 3,342,677, 3,373,156 and 3,385,847 and British Pat. Nos. 903,785, 918,169, 978,178, 991,586 and 1,033,257 and in the chemical literature by Ekstrom et al., Acta Chemica Scandinavica, 19 (2), 281-299 (1965), by A. H. Neims et al., Biochemistry (Wash) 5 (1), 203-213 (1966) and by P. Friis et al., Acta Chemica Scandinavica, l7 (9), 2391-2396 1963).

In the treatment of bacterial infections in man, the compounds of this invention are administered topically, orally and parenterlally in accordance with conventional procedures for antibiotic administration in an amount of from about 5 to mg./kg./day and preferably in the range of 15 to 50 mg./kg./day for Pseudomonas infections in divided dosages, e.g., three or four times a day. They are administered in dosage units containing, for example, 125, 250, 500, 1,000 and 2,000 mg. of active ingredient with suitable physiologically acceptable carriers or excipients. The dosage units can be in the form of liquid preparations such as solutions, dispersions, emulsions or in solid form such as tablets, capsules, etc.

The acyl isocyanates used as starting materials in the present invention are made by various methods known to the art, the most preferred of which is disclosed by Naito et al., The Journal of Antibiotics (Tokyo) Series A, 18, 145-157 (1965) and in U. S. Pat. No. 3,180,863 and the references cited therein and by Speziale and Smith, J. Org. Chem. 27, 3742-3 (1962) and J. Org. Chem. 30, 4306-7 (1965) and comprises treatment with oxalyl chloride of the corresponding amide, e.g. benzamide yields benzoyl isocyanate. An alternative method comprises treatment of an acid chloride with silver cyanate according to Billeter, Ber. 36, 3213-3221 (1903) and Hill and Degnan, J. Am. Chem. Soc. 62, 1595-6 (1940) and Naito et a1. (ibid). Another method comprises treatment of an acid chloride with cyanuric acid according to Styermark, J. Org. Chem. 28, 586 (1963).

Additional acyl isocyanates disclosed in Chemical Abstracts include the following:

The pulverized molecular sieves (Linde 4A) emis NllC1ICJI i is represented simply by ACA Thus, 7-aminocephalosporanic acid would be written These examples are given in illustration of, but not in limitation of, the present invention. All temperatures are in degrees Centigrade. Skellysolve B is a petroleum etherfraction of hp. 60-68 C. consisting essentially of n-hexane.

DESCRIPTION OF THE PREFERRED EMBODIMENTS EXAMPLE 1 000Na NH Sodium 7- D-a-[3-(2-furoyl)ureido]phenylacetamido cephalosporanate A mixture of 14.5 g. of cephaloglycin [Spencer et al., J. Med. Chem. 9, 746( 1966)], 7.2 ml. of triethylamine, 30 g. of powdered molecular sieves (Linde 4A), and 300 ml. of methylene chloride was stirred at room temperature for three hours in an apparatus protected from atmospheric moisture. The mixture was filtered to remove the molecular sieves. To the filtrate was added 5.3 g. of 2-furoyl isocyanate [Naito et al., J. Antibiotics (Tokyo), Ser. A, 18(4), -157(1965) and the mixture stirred for 1 hour at room temperature. Water ml.) was added to the reaction mixture and the methylene chloride distilled off at reduced pressure. Ethyl acetate was added to the aqueous concentrate and the mixture acidified with 42 percent phosphoric acid. The ethyl acetate phase was separated and the aqueous phase extracted twice more with ethyl acetate. Filtration was carried out during the extraction procedure to remove some insoluble material. The combined ethyl acetate extracts were washed three times with water then extracted with a solution of 4.2 g.

.of sodium bicarbonate in 150 ml. of water then twice with water. The combined bicarbonate and aqueous extracts were acidified with 42 percent phosphoric acid and extracted three times with ethyl acetate. The combined ethyl acetate extracts containing the cephalosporin free acid were washed three times with water, dried with sodium sulfate, filtered, concentrated slightly and treated with 10.7 ml. (0.03 mole) of sodium Z-ethylhexanoate in l-butanol giving a precipitate. After storage in the cold overnight the product, sodium 7-{D-u-[3-(2-furoyl)ureido]phenylacetamido} cephalosporanate, was collected by filtration and washed with ethyl acetate and acetone, giving, after trituration with 95 percent ethanol, 7 g. of crude cephalosporin sodium salt. The crude product (7 g.) was crystallized by dissolving in a small amount 2:1 water-acetone at 30 followed by cooling, giving, after drying in vacuo over phosphorus pentoxide and in vacuo at 60, 1.7 g. of sodium 7-{D-a-[3-(2-furoyl)ureido]phenylacetamido}-cephalosporanate; m.p. 189- 191 dec. with prior darkening. The infrared and nuclear magnetic resonance spectra were consistent with the desired product.

Anal. Calcd. for C H N O SNa.H O: C, H, 3.98 N, 9.62.

Found: C, 49,97; H, 4.48; N, 9.52.

The Minimum Inhibitory Concentration (M.I.C.) of this product in mcg./ml. versus a strain of Pseudomonas aeruginosa was determined by overnight incubation at 37 C. in Nutrient Broth by serial two-fold tube dilution and found to be 8-16 mcg./ml.; in the same experiment the M.I.C. for cephaloglycin was found to be 500 mcg./m1.; versus Str. pyogenes the M.l.C.s were 0.04 and 0.16 respectively.

The median curative dose (CD in mgm./kg. against an overwhelmingly lethal challenge with Str. pyogenes was determined by intramuscular injection of this product in mice of the indicated dosage at the time of challenge and 4 hours later; thus a dose of 36 mgm./kg. given at each of these two times is reported as 36 X 2. Deaths were counted for 72 hours after challenge. The CD found for this product was 7.6 X 2 m gm ./kg.; the CD for cephalothin in the same experiment was 6 X 2 mgm./kg.

EXAMPLE 2 (LOONa NII A. D(-)-a-t-Butoxycarboxamidophenylacetic acid A mixture of 30.0 g. (0.2 mole) of D(-)-2-phenylglycine and 16.0 g. (0.4 mole) of magnesium oxide powder was intimately mixed by grinding in a mortar. The mixture was suspended in 500 ml. of 50 percent aqueous dioxane and 58.0 g. (0.4 mole) of t-butoxycarbonyl azide (Commercial sample from Aldrich, t-butoxycarbonyl chloride, t-butylchlorofon'nate, is reported to be unstable above 10.) was added dropwise with vigorous stirring. The reaction mixture was heated with stirring for 20 hours at 45-50. The cooled mixture was then diluted with 2 l. of ice-water and 500 ml. of ethyl acetate with stirring. A small amount of solid was removed by filtration and the filtrate was separated into its component layers. The organic phase was extracted with 150 ml. portions of 3 percent sodium bicarbonate solution and water. These extracts were combined with the aqueous phase above and the solution was cooled and acidified to pH 5. (It is presumed that lowering the pH further would result in the liberation of hydrazoic acid.) The product was extracted into ethyl acetate (3 X 250 ml.) and the combined extracts were washed with water and dried over magnesium sulfate. Evaporation of the solvent gave an oil which was solidified by trituration with Skellysolve B" and ether. The procedure afforded 29.5 g. of white crystals of m.p. 88-90 dec.; [al -135 (C 1.0, CH OH) The mother liquors afforded a second crop of 10.5 g., m.p. 8688. Total yield 40.0 g., 80 percent.

B. 7-(D-a-Aminophenylacetamido)desacetoxyce phalosporanic acid Ethyl chloroformate (2.67 ml., 0.028 mole) was added to a stirred solution of 7.05 g. (0.028 mole) of D- a-t-butoxycarboxamidophenylacetic acid and 3.9 ml.

(0.028 mole) of triethylamine in 150 ml. of tetrahydrofuran at -5 to l0 for 15 minutes. A solution of 6 g. (0.02 mole) of 7-aminodesacetoxycephalosporanic acid [Stedman et al., J. Med. Chem. 7, ll7(l964)], 6 ml. of triethylamine, 50 ml. of water and ml. of tetrahydrofuran at 0 was added in one portion. The reaction mixture was stirred at 0 to 5 for 1 hour. An additional 100 ml. of water was added and most of the tetrahydrofuran distilled off at reduced pressure. The aqueous residue was extracted three times with ethyl acetate. The aqueous phase was acidified with 42 percent phosphoric acid and extracted with ethyl acetate, a small amount of solid being removed prior to separation of the phases. The ethyl acetate phase was washed three times with water, dried with sodium sulfate, filtered, and the solvent stripped ofl at reduced pressure. Trituration of the residue with Skellysolve B afforded 8.7 g. of 7-(D-at-butoxycarboxamidophenylacetamido)desacetoxycephalosporanic acid. This product (8.7 g.) was added to 80 ml. of trifluoroacetic acid at 10 to 15 and the solution stored at 15 for 15 minutes. The solution was poured into an ice cold mixture of 400 ml. of anhydrous ether plus 400 ml. of Skellysolve B. The precipitate of trifluoroacetate salt was collected by filtration, washed with Skellysolve B, and dried in vacuo; yield 8.3 g. A mixture of 8.3 g. of the trifluoroacetate salt, 300 ml. of water, ml. of a 25 percent solution of Amberlite LA-l resin acetate form in methyl isobutyl ketone [Spencer et al., J. Med. Chem., 9, 746(1966), footnote l4], and 140 ml. of methyl isobutyl ketone was stirred at room temperature for 3 hours. The aqueous phase was washed five times with methyl isobutyl ketone and four times with ether and filtered through diatomaceous earth (Super- Cel). The aqueous solution was concentrated to a small volume causing the product to crystallize. There was obtained 4.9 g. of 7-(D-a-aminophenylacetamido)desacetoxycephalosporanic acid. The infrared and nuclear magnetic spectra were consistent for the desired compound.

Anal. Calcd. for C H N O S.H O: C, 52.59; H, 5.24; N, 11.50.

Found: C, 52.79; H, 5.50; N, 11.24.

C. Sodium 7- {D-a-[3-(2-furoyl)ureido]phenylacetamido} desacetoxycephalosporanate A mixture of 4.7 g. of 7-(D-a-aminophenylacetamido)-desacetoxycephalosporanic acid hydrate, 2.9 ml. of triethylamine, 10 g. of powdered molecular sieves (Linde 4A). and 200 ml. of methylene chloride was stirred at room temperature for 1 hour. The molecular sieves were removed by filtration. To the filtrate was added 2.9 g. of 2-furoyl isocyanate [Naito et al., J. Antibiotics (Tokyo) set. A, 18(4), -157 (1965)]and the mixture stirred for one hour at room temperature in an apparatus protected from atmospheric moisture. Water (ca. ml.) was added to the reaction mixture and the methylene chloride was distilled off at reduced pressure. The aqueous concentrate was acidified with 42 percent phosphoric acid and twice extracted with ethyl acetate. The mixture was filtered during the second extraction to remove some insoluble material. The combined ethyl acetate extracts were washed three times with water and extracted with a solution of 4.5 g. of sodium bicarbonate in 100 ml. of

water and then twice with water. The combined bicarbonate and aqueous extracts were washed three times with ethyl acetate, acidified with 42 percent phosphoric acid, and extracted twice with ethyl acetate. The combined ethyl acetate extracts were washed three times with water, dried with sodium sulfate, filtered, and treated with 4.7 m1. (0.9135 mole) of sodium 2- ethylhexanoate in l-butanol. After storage overnight in the cold the crystalline produce was filtered, washed with ethyl acetate and acetone, and triturated with 95 percent ethanol. There was obtained, after drying for three hours at 60 in vacuo, 2.8 g. of sodium 7-{D-a-[3- (2-furoyl )ureido]phenylacetamido} -desacetoxycephalosporanate; m.p. l92194 dec. The infrared and nuclear magnetic resonance spectra were consistent for the desired compound.

The Minimum Inhibitory Concentration (M.I.C.) of this product in meg/ml. versus a strain of Str. pyogenes was determined by overnight incubation at 37 C. in Nutrient Broth by serial two-fold tube dilution and found to be 0.63 mcg./ml.; in the same experiment the M.I.C. for cephalexin was found to be 0.32 meg/ml.

The median curative dose (CD in mgm./kg. against an overwhelmingly lethal challenge with Str. pyogenes was determined by intramuscular injection of this product in mice of the indicated dosage at the time of challenge and again 4 hours later; thus a dose of 36 mgm./ kg. given at each of these two times is reported as 36 X 2. Deaths were counted for 72 hours after challenge. The CD found for this product was 90 X 2 mgrn./kg.; the CD for cephalothin in the same experiment was 6 X 2 mgm./kg.

EXAMPLE 3 OONa Nli.

Sodium 7- D-a-[ 3-( 2-thienoyl)ureido]phenylacetamido cephalosporanate A mixture of 12.2 g. of cephaloglycin, 6.2 ml. of triethylamine, 30 g. of powdered molecular sieves (Linde 4A), and 300 ml. of methylene chloride was stirred for three hours at room temperature. The mixture was filtered to remove the molecular sieves. To the filtrate was added 4.9 g. of 2-thienoyl isocyanate [Naito et al., J. Antibiotics (Tokyo), Ser. A, 18(4), 145- 157(1965)] and the mixture stirred for one hour at room temperature. Water (300 ml.) was added to the reaction mixture and the methylene chloride distilled off at reduced pressure. The aqueous residue was layered with ethyl acetate and acidified with 42 percent phosphoric acid. The mixture was filtered prior to separation to the phases to remove some insoluble material. The aqueous phase was extracted a second time with ethyl acetate. The combined ethyl acetate extracts were washed twice with water. Attempted extraction of the ethyl acetate phase with a solution of an equivalent amount of sodium bicarbonate in 300 ml. of water resulted in an unbreakable emulsion. Therefore, the whole mixture was acidified with 42 percent phosphoric acid. The ethyl acetate phase was separated, washed with water, dried with sodium sulfate, filtered, and treated with 10 ml. (0.028 mole) of sodium 2-ethylhexanoate in l-butanol giving a precipitate. After storage in the cold overnight the product was filtered, washed with ethyl acetate and sparingly with acetone, and triturated with 95 percent ethanol. The crude product was crystallized by dissolving in a minimum amount of 1:1 water-acetone at 35 and the solution filtered and cooled. There was obtained after drying in vacuo over phosphorous pentoxide and then in vacuo at 60 for two hours 0.71 g. of sodium 7-{D-a-[3-(2-thienoyl)ureido]phenylacetamido}cephalosporanate; m.p. l78-181 dec. The infrared and nuclear magnetic resonance spectra were consistent for the desired product.

Anal. Calcd. for C H N.,O S Na-2H O: C, 46.75; H, 4.09N, 9.09.

Found: C, 46.50; H, 4.65; N, 9.02.

The Minimum Inhibitory Concentration (M.I.C.) of this product in meg/ml. versus a strain of Pseudomonas aeruginosa was determined by overnight incubation of 37 C. in Nutrient Broth by serial two-fold tube dilution and found to be 16 mcg./ml.; in the same experiment the M.I.C. for cephaloglycin was found to be 500 mcg./ml.; versus Str. pyogenes the M.I.C.s were 0.04 and 0.3 respectively.

The median curative dose (CD in mgm./kg. against an overwhelmingly lethal challenge with Str. pyogenes was determined by intramuscular injection of this product in mice of the indicated dosage at the time of challenge and again 4 hours later; thus a dose of 36 mgm./kg. given at each of these two times is reported as 36 X 2. Deaths were counted for 72 hours after challenge. The CD found for this product was 11 X 2 mgm./kg.; the CD for cephalothin in the same experiment was 6 X 2 mgm./kg.

EXAMPLE 4 7- D-a-[3-(2-furoyl)ureido]phenylacetamido -3-(lpyridylmethyl)-3-cepheme-4-carboxylic acid betaine A stirred mixture of 1.4 g. of sodium 7- D-or-[3-(2- furoyl )ureido lphenylacetamido -cephalosporanate, i.. .f.p e .s m thiesrana Q-i mksf Pyridine, two ml. of water was adjusted to pH 6.5 with percent phosphoric acid and heated at 60 for 5 hours. The reaction mixture was diluted with water to a volume of about 30 ml. and extracted four times with chloroform. Residual chloroform was removed at reduced pressure. Acidification (6N hydrochloric acid) of the aqueous phase to pH 2.0 gave a white precipitate which, after drying over phosphorus pentoxide, weighed 0.9 g. This material plus 6 ml. of water and 6 ml. of a 25 percent solution of Amberlite LA-l resin acetate form in methyl isobutyl ketone was stirred for one hour. An additional 20 ml. of water and 6 ml. of resin were added and stirring continued for another hour. The reaction mixture was extracted four times with methyl isobutyl ketone. The aqueous phase was concentrated to dryness. The solid residue was triturated with anhydrous ether and filtered giving, after drying in vacuo over phosphorus pentoxide, 0.55 g. of 7- D-a-[3-(2-furoy1)ureido]-phenylacetamido -3-( 1-pyridylmethyl)- 3-cepheme-4-carboxylic acid betaine. The infrared spectrum was consistent for the desired compound.

The Minimum Inhibitory Concentration (M.I.C.) of this product in meg/ml. versus a strain of Pseudomonas aeruginosa was determined by overnight incubation at 37 C. in Nutrient Broth by serial two-fold tube dilution and found to be 32 mcg./ml.; in the same experiment the M.I.C. for cephaloridine was found to be 250 mcg./ml.

D(-)-a-t-Butoxycarboxamidophenylacetic acid A mixture of 30.0 g. (0.2 mole) of D(-)-2-phenylglycine and 16.0 g. (0.4 mole) of magnesium oxide powder was intimately mixed by grinding in a mortar. The mixture was suspended in 500 ml. of 50 percent aqueous dioxane and 58.0 g. (0.4 mole) of t-butoxycarbonyl azide (Commercial sample from Aldrich, t-butoxycarbonyl chloride, t-butylchloroformate, is reported to be unstable above 10.) was added dropwise with vigorous stirring. The reaction mixture was heated with stirring for 20 ours at 4550. The cooled mixture was then diluted with 2 l. of ice-water and 500 ml. of ethyl acetate with stirring. A small amount of solid was removed by filtration and the filtrate was separated into its component layers. The organic phase was extracted with 150 ml. portions of 3 percent sodium bicarbonate solution and water. These extracts were combined with the aqueous phase above and the solution was cooled and acidified to pH 5 (It is presumed that lowering the pH further would result in the liberation of hydrazoic acid.) The product was extracted into ethyl acetate (3 X 250 ml.) and the combined extracts were washed with water and dried over magnesium sulfate. Evaporation of the solvent gave an oil which was solidified by trituration with Skellysolve B and ether. This procedure afiorded 29.5 g. of white crystals of m.p. 88-90 dec.; [M -135 (C 1-0, CH OH). The mother liquors afforded a second crop of 10.5 g., m.p. 86-88. Total yield 400 g., 80 percent.

B. 7-[D-a-t-Butoxycarboxamidophenylacetamido ]cephalosporanic acid. (J.L. Spencer et al., J. Med. Chem, 9, 746( 1966)) A solution of 42.7 g. (0.17 mole) of D(-)-t-butoxycarboxamidophenylacetic acid and 17.2 g. (0.17 mole) of triethylamine in 600 ml. of tetrahydrofuran (THF) was cooled to 10. 18.5 g. (0.17 mole) of ethyl chloroformate was added dropwise with stirring, and the mixture was stirred for 10 min. at 10. To the mixed anhydride solution thus formed was added in one portion a cold (0) solution of 46.3 g. (0.17 mole) of 7-aminocephalosporanic acid and 17.2 g. (0.17

mole) of triethylamine in 600 ml. of 50 percent aqueous THF. The mixture was stirred for 1 hour at 0-5, and the THF was then removed under reduced pressure. (Any solid material at this stage should be removed by filtration.) The residue was dissolved in a mixture of 1 l. of cold water and 400 ml. of ethyl acetate, and after a brief shaking the layers were separated. The aqueous phase was cooled, layered with ethyl acetate and 42 percent phosphoric acid was added to pH 3 with stirring. The phases were separated and an extraction was made with fresh ethyl acetate. The combined extracts were washed with cold water, dried over magnesium sulfate and the solvent was removed under reduced pressure. After trituration with ether and Skellysolve B the residual oil solidified to give 62.5 g. (72.5 percent) of 7-[D-a-t-butoxycarboxamidophenylacetamido]cephalosporanic acid.

7-[D(-)-a-Aminophenylacetamido]ce phalosporanic acid, cephaloglycin A solution of 13.5 g. of the derivative described above in 400 ml. of 45 percent formic acid was stored at 40 for 3 hours. The solvent was then removed under reduced pressure, and the last traces of formic acid were removed by azeotropic distillation under reduced pressure with toluene. The oily residue was treated with ml. of ethyl acetate plus 5 ml. of water, which caused solidification. The solid was triturated with ether and collected by filtration. After drying in vacuo over P 0 there was obtained 10.0 g. (88.5 percent) of crystalline cephaloglycin, [a] +8l (@1'0, 50 percent aqueous acetonitrile).

D. Sodium 7-[D-a-(3-benzoylureido)phenylacetamido]cephalosporanate A mixture of 4.2 g. of cephaloglycin, 2.1 ml. of triethylamine, and ml. of methylene chloride was stirred for 10-15 minutes at room temperature. Benzoyl isocyanate (2.9 g.) [Speziale, Smith, J. Org. Chem. 27, 3742(1962)] was added in one portion and the reaction mixture stirred for 1 hour at room temperature. To the filtered reaction mixture was added about ml. of water and the methylene chloride stripped off at reduced pressure. The aqueous residue was layered with ethyl acetate and acidified with 42 percent phosphoric acid. Two more extractions with ethyl acetate were made on the aqueous phase. The combined ethyl acetate extracts were washed twice with water and then extracted with a solution of one equivalent of sodium bicarbonate in 150 ml. of water followed by two extractions with water. The combined aqueous bicarbonate extracts were acidified with 42 percent phosphoric acid and extracted three times with ethyl acetate. The combined ethyl acetate extracts were washed twice with water, dried with sodium sulfate, filtered, and treated with 3.5 ml. (0.01 mole) of sodium Z-ethylhexanoate in l-butanol giving a precipitate. After storage overnight in the cold, the crystalline product was collected by filtration and washed with ethyl acetate; yield 4.2 g. The product was recrystallized by dissolving in 95 percent ethanol plus sufficient water to dissolve most of the material (a small amount of insoluble material was removed by filtration) followed by dilution with ethyl acetate and cooling. After drying in vacuo over phosphorus pentoxide and in vacuo at 60 for three hours there was obtained 2.36 g. of sodium 7-[D-a-(3-benzoylureido)-2- phenylacetamido]cephalosporanate; m.p. 165-167 dec. The infrared and nuclear magnetic resonance spectra were consistent for the desired compound.

The Minimum Inhibitory Concentration (M.I.C.) of this product in mcg./ml. versus a strain of Pseudomonas aeruginosa was determined by overnight incubation at 37 C. in Nutrient Broth by serial two-fold tube dilution and found to be 16-32 mcg./ml.; in the same experiment the M.I.C. for cephalothin was found to be 250 mcg./ml.

EXAMPLE 6 I benzoylureidol phenylacetamido]-cepha1osporanate,

8.1 g. of potassium thiocyanate, 1.5 ml. of pyridine, and 6-10 ml. of water was adjusted to pH 6.5 with 42 percent phosphoric acid and heated at 60 for 5 hours. The reaction mixture was diluted with water and extracted with chloroform, a quantity (4.8 g.) of insoluble material (solid A) being removed by filtration. The aqueous phase was extracted four additional times with chloroform and any residual chloroform removed at reduced pressure. The aqueous solution was adjusted to pH 2.0 giving a solid which was filtered, washed with water, and air dried (solid B); yield 0.55 g. Solid A was again treated with pyridine and potassium thiocyanate as above giving recovered solid A and 0.3 g. more of solid B on adjusting the aqueous phase to pH 2.0. An aqueous suspension of recovered solid A was adjusted to pH 2.0. After stirring the product was filtered and washed with water. This material was identical with solid B; yield 2.6 g. The combined crops of solid B (3.5 g.) were stirred for 2% hours at room temperature with 30 ml. of water and 30 ml. of a 25 percent solution of Amberlite LA-l resin acetate form in methyl isobutyl ketone [Spencer et al., J. Med. Chem. 9,746( 1966), footnote 14]. The crystalline product was filtered and washed with methyl isobutyl ketone.

Recrystallization from dimethylacetamide-water afforded, after drying in vacuo at 65 for 3 hours, 0.23 g. of 7-[D-a-(3-benzoylureido)phenylacetamido]-3-( 1- pyridylmethyl)-3-cepheme-4-carboxylic acid betaine; m.p. 170l 80 dec. The infrared and nuclear magnetic resonance spectra were consistent for the desired compound.

Anal. Found: C, 54.91; H, 5.41; N, 11.49; H 0, 9.1. Calcd. for C l-l N S.3l- 0: C, 55.67; H, 5.00; N, 11.20; H 0, 9.46.

The Minimum Inhibitory Concentration (M.I.C.) of this product in mcgJml. versus a strain of Pseudomonas aeruginosa was determined by overnight incubation at 37 C. in Nutrient Broth by serial two-fold tube dilution and found to be 8-16 mcg./ml.; in the same experiment the M.I.C. for each of cephaloridine and cephalothin was found to be 250 meg/ml.

The median curative dose (CD in mgmJkg. against an overwhelmingly lethal challenge with Str. pyogenes was determined by intramuscular injection of this product in mice of the indicated dosage at the time of challenge and again 4 hours later; thus a dose of 36 mgm./kg. given at each of these two times is reported as 36 X 2. Deaths were counted for 72 hours after challenge. The CD,,., found for this product was 0.68 X 2 mgm./kg.; the CD for cephalothin in the same experiment was 5 X 2 mgm./kg.

EXAMPLE 7 Sodiumv 7-[D-a-(3-benzoylureido)-2- thienylacetamido]-cephalosporanate A mixture of 1.8 g. of 7-(D-a-amino-2- thienylacetamido)cephalosporanic acid, one ml. of triethylamine, and ml. of methylene chloride was stirred at room temperature for 15 minutes. Benzoyl isocyanate (2.5 ml.) [Speziale, Smith, J. Org. Chem, 27, 3742(1962)]was added in one portion and the resulting dark colored solution stirred for 1 hour at room temperature. Water was added and the methylene chloride stripped off at reduced pressure. Ethyl acetate was added to the aqueous concentrate and the mixture acidified with 42 percent phosphoric acid. Two additional extractions were made with ethyl acetate. The combined ethyl acetate extracts were washed three times with water and extracted with a solution of 1.5 g. of sodium bicarbonate in ca. 100 ml. of water and twice with water. The combined aqueous bicarbonate extracts were washed three times with water, dried with sodium sulfate, filtered, and treated with 1.4 ml. (0.0039 mole) of sodium 2-ethylhexanoate in l-butanol giving a precipitate. After concentrating slightly, fresh ethyl acetate was added and the product sodium 7-[D-a-( 3-benzoylureido)-2-thienylacetamido] cephalosporanate collected by filtration and washed with ethyl acetate; yield 1.1 g. The infrared spectrum was consistent for the desired compound.

EXAMPLE 8 o @T1r i1i o x-cm0 c om NH LOONa O:ONH-CCHzCIIa Sodium 7-[D-a-(3-propionylureido)phenylacetamido ]cepha.losporanate A mixture of 4.2 g. of cephaloglycin, 2.1 ml. of triethylamine and 100 m1. of methylene chloride was stirred for 15 minutes at room temperature. Propionyl isocyanate (1.98 g.) (Naito et al., .1. Antibiotics (Tokyo), Ser. A, 18 (4), -157 (1965)) was added slowly and the mixture stirred for one hour at room temperature. Water ml.) was added to the filtered reaction mixture and the methylene chloride distilled off at reduced pressure. The aqueous concentrate was layered with ethyl acetate and acidified with 42 percent phosphoric acid. The aqueous phase was extracted twice more than ethyl acetate. The combined ethyl acetate extracts were washed twice with water and extracted with a solution of one equivalent of sodium bicarbonate in 100 ml. of water followed by two extractions with water. The combined bicarbonate and aque' ous extracts were layered with ethyl acetate and acidified with 42 percent phosphoric acid. After two additional extractions the combined organic phases were washed three times with water and dried with sodium sulfate. The drying agent was removed by filtration and the filtrate treated with 3.5 ml. (0.01 mole) of sodium Z-ethylhexanoate in l-butanol, precipitating the crystalline sodium salt. The product was collected by filtration and washed with ethyl acetate; yield 2.0 g. The product, sodium 7-[D-a-(3-propionylureido)phenylacetamido]-cephalosporanate, was recrystallized by dissolving in a minimum amount of 1:1 acetone-water, filtering and adding acetone to near the cloud point; yield 0.85 g., mp. 16 l l 64 dec. with prior darkening. The infrared and nuclear magnetic resonance spectra were consistent for the desired compound.

Anal. Found: C, 46.74; H, 4.76; N, 9.98.

Calcd. for C H N SNa2H 0: C, 46.97; H, 4.84; N, 9.96. The Minimum Inhibitory Concentration (M.l.C.) of this product in mcg./ml. versus a strain of Pseudomonas aeruginosa was determined by overnight incubation at 37 C. in Nutrient Broth by serial two-fold the dulution and found to be 63 mcg./ml.; in the same experiment the M.l.C. for cephalothin was found to be 500 mcg./ml.

EXAMPLE 9 LOOK Potassium 7-[D-a-(3-acetylureido)phenylacetamido] cephalosporanate A. Preparation of acetyl isocyanate Acetyl chloride (60 g.) was added dropwise to a stirred suspension of 125 g. of dry silver cyanate in 250 ml. of dry n-pentane with cooling to maintain the temperature at to The mixture was refluxed for one-half hour and then stirred at room temperature for another one-half hour. The organic phase was decanted from the solid residue and added dropwise to 50 g. of silver cyanate with good stirring; the mixture was allowed to reflux from the heat of reaction during the addition. After stirring for one hour at room temperature an infrared spectrum of the organic phase showed the presence of acetyl isocyanate plus some acetyl chloride. Therefore, an additional 20 g. of silver cyanate was added and the mixture stirred for one-half hour. The organic phase was decanted from the solid residue. An infrared spectrum showed the solution to contain approximately 3 percent acetyl isocyanate and no acetyl chloride; volume 200 ml.

B. Reaction with cephaloglycin Triethylamine (10.5 ml., 0.075 mole) is added to a stirred suspension of 0.05 mole of cephaloglycin in 600 ml. of methylene chloride. Powdered molecular sieves (Linde 4A) (45 g.) are added and the mixture stirred for 3 hours at room temperature in an apparatus protected from atmospheric moisture. The molecular sieves are removed by filtration with an additional ml. (approximately) of methylene chloride being used to wash the filter cake. The above-prepared solution of acetyl isocyanate in n-pentane (200 ml., about 6 g., 0.0707 mole of acetyl isocyanate) is added to the thus obtained solution of cephaloglycin triethylammonium salt in methylene chloride. The solution is stirred for 3 hours at room temperature in an apparatus protected from atmospheric moisture. The reaction mixture is extracted five times with water. The combined aqueous extracts are washed three times with ethyl acetate. The aqueous phase is acidified with 42 percent phosphoric acid and extracted with a total of 800 ml. of ethyl acetate in three portions. The combined ethyl acetate extracts are washed three times with water, dried (anhydrous sodium sulfate), filtered, and treated with 18 ml. (0.05 mole) of potassium 2-ethylhexanoate in l-butanol. An oil separates which crystallizes on seeding. After one-half hour the mixture is concentrated slightly on the rotary flash evaporator and the product, potassium 7-[D-a-( 3-acetylureido)phenylacetamido]- cephalosporanate, collected by filtration, washed with ethyl acetate and acetone, dried overnight in vacuo over phosphorus pentoxide and further dried for two hours in a vacuum oven at 6065.

EXAMPLE 10 O a TH- i-AGA CHQO-d-CHS NH 100M Sodium 7-[D-a-(3-chloroacetylureido)phenylacetamido]cephalosporanate Triethylamine (11.5 ml., 0.0744 mole) is added to a suspension of 0.0496 mole of cephaloglycin in ml. of methylene chloride. After stirring for 10 minutes 30 g. of powdered molecular sieves (Linde 4A) are added and the mixture is stirred for three hours at room temperature. The molecular sieves are removed by filtration with an additional 30 ml. of methylene chloride being used to wash the filter cake.

To the thus obtained solution of cephaloglycin triethylammonium salt in methylene chloride is added 6.0 g. (0.050 mole) of chloroacetyl isocyanate [Speziale, Smith, J. Org. Chem. 27, 3742 (1962)] and the solution is stirred for one hour at room temperature in an apparatus protected from atmospheric moisture. The reaction mixture is extracted three times with water. The combined aqueous extracts are washed once with ethyl acetate. The aqueous phase is acidified with 42 percent phosphoric acid and extracted three times with ethyl acetate. The combined ethyl acetate extracts containing the cephalosporin free acid are washed three times with water, dried (anhydrous sodium sulfate), filtered, concentrated to a volume of about 250 ml., and treated with 16.2 ml. (0.049 mole) of sodium 2-ethylhexanoate in l-butanol giving a precipitate of sodium 7-[D-a-(3-chloroacetylureido)phenylacetamido]cephalosporanate which is collected by filtration, washed with ethyl acetate and acetone and dried in vacuo over phosphorous pentoxide.

EXAMPLE 11 Potassium 7-[ D-a-( 3-acetylureido )-3- thienylacetamido]cephalosporanate 7-(D-a-Amino-3 thienylacetamido)cephalosporanic acid (0.0244 mole), 5.1 ml. (0.0366) of triethylamine, 25 g. of powdered molecular sieves (Linde 4A) and 300 ml. of methylene chloride are combined and stirred at room temperature for 3 hours. The molecular sieves are removed by filtration, an additional 50 ml. of methylene chloride being used to wash the filter cake. To the filtrate is added 130 ml. of approximately a 3 percent solution of acetyl isocyanate in n-pentane. The solution is stirred for 1.5 hours at room temperature and then extracted four times with water. The combined aqueous extracts are washed three times with ethyl acetate, acidified with 42 percent phosphoric acid, and extracted with 3 portions of ethyl acetate. The combined ethyl acetate containing the cephalosporin free acid are washed three times with water, dried with sodium sulfate, filtered, concentrated slightly, and treated with 8.9 ml. (0.0244 mole) of potassium Z-ethylhexanoate in l-butanol to give an oil which crystallizes. The product, potassium 7-[D-a-(3- acetylureido)-3-thienylacetamido]cephalosporanate, is collected by filtration and washed with ethyl acetate and acetone.

EXAMPLE l2 Potassium 7-[D-a-(3-phenylacetylureido)phenylacetamido]cephalosporanate A mixture of 0.056 mole of cephaloglycin, 11.8 ml. (0.084 mole) of triethylamine, 30 g. of powdered molecular sieves, and 300 ml. of methylene chloride is stirred for 3 at room temperature. The molecular sieves are removed by filtration. Phenylacetyl isocyanate [Speziale, Smith, J. Org. Chem., 27, 3742 (1962)] (9.99 g., 0.062 mole) is added and the mixture stirred at room temperature for 1 hour. Water is added. The methylene chloride was stripped off at reduced pressure and the aqueous phase is washed three times with ethyl acetate. The aqueous phase is layered with ethyl acetate, acidified with 42 percent phosphoric acid, and extracted twice more with ethyl acetate. The combined ethyl acetate extracts are washed three times with water, dried (sodium sulfate), filtered, and treated with 20.4 ml. (0.056- mole) of potassium 2-ethylhexanoate in l-butanol. The crystalline product, potassium 7-[D- a-( 3phenylacetylureido)phenylacetamido]- cephalosporanate, is collected by filtration, washed with ethyl acetate and sparingly with acetone, dried in vacuo over phosphorus pentoxide and further dried for 2-3 hours in a vacuum oven at 65.

EXAMPLE 13 p o (IHCACA-CH2O%CH3 (I30 ONa Sodium 7-[D-a-(3-nicotinoylureido)phenylacetamido ]cephalosporanate To a suspension of 12.2 g. (0.1 mole) of nicotinamide in ml. of ethylene dichloride is added 17.5 g. (1 1.7 ml.) of oxalyl chloride and the mixture is refluxed for 18 hours. The solvent is decanted and the solid, resinous residue is washed four times with methylene chloride; yield 14 g.

A mixture of 0.025 mole of cephaloglycin, 19.3 ml. (0.138 mole) of triethylamine, 20 g. of powdered molecular sieves and 400 ml. of methylene chloride is stirred at room temperature for 3 hours. The molecular sieves are removed by filtration. To the filtrate is added the 14 g. of product obtained from the reaction of nicotinamide with oxalyl chloride. The solution is stirred at room temperature for 1 hour. Water (250 ml.) is added and the methylene chloride removed at reduced pressure. The aqueous residue is adjusted to pH 8 with sodium bicarbonate and washed twice with ethyl acetate. The aqueous phase is layered with ethyl acetate and adjusted to pH 4.5 with 6 N hydrochloric acid. Two more extractions are made on the aqueous phase with ethyl acetate. The combined ethyl acetate extracts are washed twice with water, dried with sodium sulfate, filtered and treated with 8.4 g. of a 50 percent solution of sodium 2-ethyl-hexanoate in l-butanol. After concentrating to a small volume the remaining ethyl acetate is decanted and the residue triturated with anhydrous ether. The product, sodium 7-[D-a-(3- nicotinoylureido)phenylacetamido]cephalosporanate, is dissolved in wet ethanol and reprecipitated with ethyl acetate.

EXAMPLE l4 Substitution of an equal weight of Z-pyridine-carboxylic acid amide and 4-pyridinecarboxylic acid amide, respectively, for the nicotinamide in the procedure of Example 13 produces sodium 7-[D-a-(2-nicotinoylureido)phenylacetamido]-cephalosporanate and sodium 7-[D-a-(4 nicotinoylureido)-phenylacetarnido]cephalosporanate, respectively.

EXAMPLE 15 TH-C-ACA-CHzO CH3 I S TH C O ONa EXAMPLE 16 Replacement of the 2-furoyl isocyanate of Examples 1 and 2 with an equimolar weight of 5-nitro-2-furoyl isocyanate produces sodium 7-{D-a-[3-(5-nitro-2-furoyl)ureido]phenyl-acetamido}cephalosporanate and sodium 7- {D-a-[ 3-( 5 nitro-2-furoyl)ureido1phenylace tamido}desacetoxycephalosporanate respectively.

5-Nitro-2-furoyl isocyanate is prepared according to Naito et a1. (ibid, Example 1) from 5-nitro-2-furoic acid amide (Bell, 18, 288).

EXAMPLE 17 The 2-furoyl isocyanate of eachof Examples 1 and 2 is replaced by an equimolar weight of the aroyl isocyanate prepared by the method-of Speziale and Smith [J. Org. Chem. 27, 3742-3 (1962)] from the corresponding aroyl amide of the followingtable:

Amide Illustrative sources N: H2 Annde: commercially available. N

CON

WCONH:

Amide, acid: Beil. 27, 707. Acid chloride:

readily prepared by known methods. N N

Acid, acid chloride: Doyle and Nnylor, CONH2 U.S. 2,996,501 and references cited I erein. N

O CH:

HaC- 'CONH2 Acid, acid chloride: Doyle and Nayler, 2,996,501 and references cited to produce, respectively, the compounds of the formulae:

wherein Z is:

When necessary the amide is prepared by converting the corresponding acid to its acid chloride with thionyl chloride and 'thenceto the amide by treatment of the acid chloride with ammonia in the usual manner.

EXAMPLE 18 The benzoyl isocyanate of Example 7 and the acetyl isocyanate of each of Examples '9 and l1 are each replaced by an equimolar weight of the acyl isocyanate of the formula wherein R is dichloromethyl, trichloro'rnethyl, npropyl, isopropyl, n-butyl, isobutyl, sec.-butyl, t-butyl, n-pentyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl, respectively to produce, respectively, the corresponding compounds of the formulas and NH J

The acyl isocyanates are prepared according to 'Naito et al., (ibid) or from the amides of the formula R CONH according to Speziale and Smith (ibid).

D-a-amino-p-iodophenylacetic acid,

D-a-amino-m-iodophenylacetic acid,

D-a-amino-m-chloro-p-hydroxyphenylacetic acid,

D-a-arnino-p-methoxyphenylacetic acid.

D-a-amino-p-hydroxyphenylacetic acid,

D-a-amino-m-methoxyphenylacetic acid,

D-oz-amino-m-hydroxyphenylacetic acid,

D-a-amino-p-acetamidophenylacetic acid,

D-a-amino-m-aminophenylacetic acid, and

D-a-amino m-acetamidophenylacetic acid, respectively, produces sodium 7-[ D-a-( 3-benzoylureido)-2- thienylacetamido]cephalosporanate,

sodium 7-[ D-a-( 3-benzoylureido )-3- thienylacetamido]cephalosporanate,

sodium 7-[D-a-(3-benzoylureido)-m-nitrophenylacetamido]cephalosporanate,

sodium 7-[D-a-(3-benzoylureido)-m-aminophenylacetamido]cephalosporanate,

sodium 7-[DL-a-(3-benzoylureido)-p-methylphenylacetamido]cephalosporanate,

sodium 7-[DL-a-(3-benzoylureido)-m-methylphenylacetamido]cephalosporanate,

sodium 7-[DL-a-(3-benzoylureido)-p-chlorophenylacetamido]cephalosporanate,

sodium 7-[DL-a-( 3-benzoylureido )-m-chlorophenylacetamido]cephalosporanate,

sodium 7-[ DL-a-( 3-benzoylureido)-p-methoxyphensodium 7-[DL-a-(3-benzoylureido)-m-fluorophenylacetamido cephalosporanate,

sodium 7- DL-a-( 3benzoylureido)-p-hydroxyphenylacetamido cephalosporanate,

sodium 7-[ DL-a-( 3-benzoylureido )-m-hydroxyphenylacetamido cephalosporanate,

sodium 7-[DL-a-( 3-benzoylureido)-p-aminophenylacetamido ]cephalosporanate,

sodium 7-[ DL-a-( 3-benzoylureido )-m-aminophenylacetamido ]cephalosporanate,

sodium 7- DL-a-( 3-benzoylureido )-m-nitrophenylacetamido ]cephalosporanate,

sodium 7- DL-a-( 3-benzoy1ureido)-pdimethylaminophenylacetamido]cephalosporanate.

ylacetamido ]cephalosporanate,

sodium 7-[ D-a-( 3benzoylureido )-p-acetamidophenylacetamido]cephalosporanate,

sodium 7-[ D-a-( 3-benzoylureido-m-aminophenylacetamido]cephalosporanate and sodium 7-[D-a-( 3-benzoylureido )-macetamidophenylacetamido] -cephalosporanate respectively.

The preparation of each of these a-amino acids is described in either U. S. Pat. Nos. 3,198,803 and 3,342,677 or by Friis et al., Acta Chem. Scand. 17, 2391-2396(1966) or by Neims et al., Biochemistry (Wash) 5, 203-213(1966) or in the section below entitled Illustrative Preparations of Starting Reagents.

Each of these a-amino acids is also converted to the corresponding substituted cephaloglycin by each of the two general procedures described by Spencer et al., J. Med. Chem. 9(5), 746-750(1966) and references cited therein which involve the use of an N-p-nitrobenzyloxy carbonyl protecting group and a B-dicarbonyl protecting group, respectively. For the latter, methyl acetoacetate is preferred.

Substitution in the procedure of Example 6 for the sodium 7-[D-a-(3-benzoylureido)phenylacetamido] cephalosporanate used therein of an equimolar weight of each of the above products produces the cor- 0 responding betaine.

lLLUSTRATIVE PREPARATIONS OF STARTING REAGENTS A. Ring-substituted 2Phenylglycines Substituted DL Z-phenylglycines are prepared by alkaline hydrolysis of the appropriate S-arylhydantoins which in turn are prepared from substituted benzaldehydes by the method of Bucherer and Leib, J. Prakt. Chem., 141, 5(1934); for additional examples of this procedure see also U.S. Pat. No. 3,140,282. The substituted DL 2-pheny1glycines are resolved, if desired,

via their N-formyl derivatives as described by E. Fisher et al., Ber. 41, 1286(1908) or by one of the procedures illustrated below.

D-a-acetamido-phenylacetic acid. A suspension of 50 g. (0.331 mole) of D-(-)-2-phenylglycine in 700 ml. of water was cooled to 0 to 5 C. and 13.2 g. (0.331 mole) of sodium hydroxide was added with stirring to produce a solution. Acetic anhydride (67.5 g., 0.662 mole) was added rapidly in one portion to the vigorously stirred solution which was initially cooled to 0 to 5 C. by means of a salt-ice cooling bath. This was immediately followed by the addition of a solution of 39.7 g. (0.993 mole) of sodium hydroxide in 200 ml. of water in a rapid stream from a dropping funnel. The temperature rose to a maximum of about 25 C. The solution was stirred for an additional 15 minutes in the cooling bath and then acidified with concentrated hydrochloric acid. The precipitated product was collected by filtration, washed on the filter with water and recrystallized from 1:1 percent ethanol-water; yield 46.0 g. (72%), m.p. 186188 C., [al =*217.9 (C lpercent, ethanol).

D-a-acetamido-4-nitrophenylacetic acid D-a-acetamidophenylacetic acid (20 g., 0.104 mole) was slowly added to 50 ml. of concentrated sulfuric acid with cooling as needed to maintain the temperature at 20 to 25 C. The mixture was stirred for about 20 minutes until most of the solid dissolved. Nitric acid (90%, d 1.5, 9.7 ml. 0.208 mole) was added dropwise at such a rate to the stirred mixture that the salt-ice cooling bath maintained the temperature in the range to C. The reaction mixture was stirred at --5 to C. for an additional 30 minutes and then poured onto about 300 g. of ice flakes. The white crystalline product was collected by filtration, washed with water and recrystallized three times from 1:1 95% ethanolwater; m.p. l80-182 C. dec., yield 11.5 g. (46.4 percent). An additional recrystallization from ethyl acetate did not change the melting point; [60 h? 206.4 (C 5%, ethanol).

Anal. Calcd. for C H N O C, 50.42; H, 4.23; N, 11.76. Found: C, 50.14; H, 4.07; N, 11.96.

D-a-acetamido-4-aminophenylacetic acid A solution of g. (0.063 mole) of D-a-acetamido- 4-nitrophenylacetic acid in 250 ml. of 95 percent ethanol was hydrogenated in the presence of 0.6 g. of 5 percent palladium on carbon on a Paar hydrogenator at an initial pressure of 50 p.s.i. for 64 minutes. The product had crystallized from the hydrogenation mixture. Approximately 200 ml. of water was added, the mixture warmed to dissolve the product and the catalyst removed by filtration. Chilling the filtrate gave 9.9 g. of product, m.p. 192 195 C. dec. The product was recrystallized four times from 1:1 95 percent ethanol-water, weight 4.8 g., m.p. 207-209 C. dec., [al =182.2 (C= 0.5 percent, 1 N HCL).

Anal. Calcd. for C H N Q z C, 57.71; H, 5.81; N, 13.46. Found: C, 57.61, 57.64; H, 5.67;N, 13.18.

D-a-Acetamido-4-iodophenylacetic aciL V To a solution of 5.0 g. (0.024 mole) of D-aacetamido-4-aminophenylacetic acid in 70 ml. of trifluoroacetic acid at -5 to 0 was added slowly 1.8 g. of sodium nitrite. The solution was stirred for 25 minutes. Solid potassium iodide (4.8 g., 0.024 mole) was added at 0 to 5. The temperature of the dark brown mixture was increased to 30 whereupon a vigorous gas evolution occurred. The mixture was maintained at 30 for 45 minutes and then heated at reflux for one-half hour. The trifluoracetic acid phase was decanted from the dark colored insoluble material. The trifluoroacetic acid was distilled ofl at reduced pressure. The residue was taken up in 50 ml. of water. After ice cooling there was obtained a precipitate of brown solid. Two recrystallizations'from 1:1 95 percent ethanol-water gave D-a-acetamido- 4-iodophenylacetic acid; m.p. 217 dec. with darkening at 202, [01] 173.2 (C 0.5, 95 percent ethanol).

Anal. Calcd. for C H INO C, 37.64; H, 3.16; N, 4.39. Found: C, 37.84; H, 3.30; N, 4.34.

The dark colored insoluble material was slurried with water and treated with 1 M sodium thiosulfate to remove the iodine color. The solid was filtered, washed with water and twice recrystallized from 1:1 95 percent ethanol-water with a carbon treatment giving additional product: [ab l70.6 (C=0.5, 95 percent ethanol).

Anal. Calcd, for c,,H, INo,: C, 37.64; H, 3.16; N, 4.39. Found: C, 37.70; H, 3.2.5; N, 4.45.

D-a-Amino-4-iodophenylacetic acid A suspension of 3.7 g. (0.011 mole) of D-aacetamido-4-iodophenylacetic acid in 15 ml. of 2 N hydrochloric acid plus sufficient dioxane to give a solution at the boiling point was heated at reflux for 1.5 hours. The solvent was distilled off at reduced pressure. The residue was extracted with water, the insoluble material (solid A) being removed by filtration. The filtrate was stripped to dryness at reduced pressure and the solid residue was extracted with water, the insoluble material (solid B) again removed. The filtrate was again evaporated to dryness and the residue extracted with water and the insoluble material (solid C) again removed. The filtrate was stripped to dryness giving solid D as residue. The infrared spectra (KBr) showed solids A and B to be amino acid zwitter ion and solid C to be mostly amino acid hydrochloride.

Solid A was hydrolyzed in 2.5 N hydrochloric acid plus dioxane for 1.75 hours. The solution was evaporated to dryness, the residue taken up in water, a small amount of insoluble material removed by filtration, and the filtrate evaporated to dryness leaving solid E. An infrared spectrum (KBr) showed solid E to be a mixture of amino acid hydrochloride and zwitter ion.

Solids D and E were combined in water and the system adjusted to pH 4.5 giving 1.55 g. of D-a-amino- 4-iodophenylacetic acid; m.p. 204-205 dec., [a],, =99.4 (C=0.5, l N HCL).

Anal. Calcd. for C H INO C, 34.68; H, 2.91; N, 5.06. Found: C, 34.63; H, 3.24; N, 4.77.

Drei -i 9p s a st s= s D-a-Acetamidophenylacetic acid (Beil. 14, 591) (200 g., 1.036 mole) was added slowly to a solution of 161.6 g. (0.52 mole) of silver sulfate in 1.2 l. of conc.

sulfuric acid with cooling as needed to keep the temperature below 30. Finely pulverized iodine (684 g., 2.7 mole) was added in portions during 1.5 hours. The mixture was stirred at room temperature for 1.5 hours longer. The mixture was filtered through a sintered glass filter and the filtrate poured into ca. 3 1. of crushed ice. The solid was filtered, washed with water, and air dried. The material was recrystallized from 650 ml. of 2-propanol (the hot solution was filtered to remove some insoluble material) giving solid A; yield 46.6 g., m.p. ll83 dec. The filtrate was concentrated and stored in the cold overnight giving solid B; yield 132 g., m.p. l68. Solids A and B were crude D-a-acetamido-4-iodophenylacetic acid.

Solid B was combined with 500 ml. of 2 N hydrochloric acid and refluxed for one hour. The insoluble material (solid C) was removed by filtration and washed with water; yield 100 g., m.p. -183.

Solid C was hydrolyzed in 200 ml. of 2 N hydrochloric acid plus enough dioxane to solubilize the material. After 2.25 hours at reflux the solvent was distilled off at reduced pressure and the residue extracted with 250 ml. of water. The insoluble material (solid D) was removed by filtration. The filtrate was adjusted to pH 4.5 and after cooling in an ice bath the precipitate was filtered, washed with water, and triturated with boiling 95 percent ethanol giving 10.8 g. of D-a-amino-4- iodophenylacetic acid. g A

Solid A was hydrolyzed in 2 N hydrochloric acid plus dioxane for 2 hours and the solvent distilled off at reduced pressure. The residue was extracted with water. The insoluble material (solid F) was removed by filtration. The filtrate was adjusted to pH 4.5 giving crystalline D-04amino-4-iodophenylacetic acid; yield 14.4 g., [01],, 32 86.2 (C =0.5, l N HCL).

Solids D and F were combined and suspended in 350 ml. of water. The suspension was adjusted to pH 4.5 with 20 percent sodium hydroxide. The solid was filtered, washed with water, air dried, and triturated with 300 ml. of boiling 95 percent ethanol giving 42.5 g. of D-a-amino-4-iodophenylacetic acid; [a],,' 99.8 (C 0.5,1 N HCL).

D-a-Amino-4-iodophenylacetyl hydrochloride A suspension of 42.3 g. (0.15 mole) of finely ground D-a-amino-4iodophenylacetic acid in 1.5 l. of methylene chloride was gassed at to with anhydrous hydrogen chloride and 40.6 g. (0.195 mole) of phosphorus pentachloride added. The mixture was stirred for 2 hours at 5. Skellysolve B (800 ml.) was added to the reaction mixture and the product collected by filtration. The product was washed with Skel lysolve B and dried in vacuo; yield 40.9 g. (82 percent).

D-a-Acetamido 3-iodophenylacetic acid.

To a solution of 50.0 g. (0.24 mole) of D-aacetamido-3-aminophenylacetic acid in 550 ml. of trifluoroacetic acid at 5 was added 17.0 g. of 97 percent sodium nitrite gradually during minutes. The solution was stirred at 5 for 25 minutes longer. The diazonium salt solution was added in a steady stream to a vigorously stirred suspension of 79.0 g. of potassium iodide and 2.5 g. of iodine in 300 ml. of trifluoroacetic acid initially at 23. During the addition the temperature rose to 2527 and steady gas evolution was noted. The mixture was stirred for 3.5 hours at room temperature until the gas evolution ceased. The reaction mixture was filtered leaving a quantity of dark gummy solid. The filtrate was concentrated to a small volume, water added, and further concentrated. The concentrate containing a solid was treated with dilute sodium thiosulfate and the solid collected by filtration. Recrystallization from 4:1 water 95 percent ethanol gave 19.5 g. of D-a-acetamido-3-iodophenylacetic acid; m.p. 18l-181.5, [a],," l58.0 (C 0.5,95 percent ethanol).

Anal. Calcd. for C H INO C, 37.64; H, 3.16; N, 4.39; I, 39.77. Found: C, 37.80; H, 3.07; N, 4.55; I,

D-a-Amino3iodophenylacetic acid D-a-Acetamido-3-iodophenylacetic acid (10.0 g.) in 45 ml. of 2 N hydrochloric acid plus sufficient dioxane to give a solution at the boiling point was refluxed for 2.25 hours. The solvent was evaporated to dryness and the residue extracted with water. The insoluble material (solid A) was removed by filtration. The filtrate was evaporated to dryness and the residue in water was adjusted to pH 4.5 with sodium hydroxide giving 1.0 g. of D-a-amino 3-iodophenylacetic acid; m.p. l92-195, [11],, =8l (C=0.5, l N HCL).

The filtrate deposited a second crop of amino acid on storage in the cold; yield 0.6 g., m.p. 203204.5, [a] =l01.4(C=0.5, l N HCL).

Solid A (which was chiefly amide) was hydrolyzed with 45 ml. 2 N hydrochloric acid plus dioxane for 2 chloride hours at reflux. The residue remaining after evaporation of the solvent was combined with water and again evaporated to dryness. The residue in water was adjusted to pH 4.5 giving 1.9 g. of D-a-amino-3- iodophenylacetic acid; m.p. l96-l99, [01],, 95 (C=0.5, l N HCL).

The infrared and nuclear magnetic resonance spectra of the three fractions were consistent with the desired product.

D-a-Amino-3iodophenylacetyl hydrochloride I A suspension of 2.5 g. (0.009 mole) of D-a-amino-B- iodophenylacetic acid in 100 ml. of methylene chloride at 0 to 5 was gassed with anhydrous hydrogen chloride and 2.5 g. (0.012 mole) of phosphorus pentachloride added. After stirring for 24 hours at 0 to 5 an additional 1.2 g. of phosphorus pentachloride was added and stirring continued for a total of 38 hours. The reaction mixture was diluted with Skellysolve B, the product filtered, washed with Skellysolve B, and dried in vacuo; yield 1.2 g.

D-(-)-a-Amino-a-(3-chloro-4-hydroxyphenyl)glycine To a stirred suspension of 5.01 g. (0.03 mole) of D-(- )-2-(p-hydroxypheny1)glycine in 100 ml. of glacial acetic acid was bubbled in HCl gas at a vigorous rate for about 5 minutes. At first a clear solution resulted and then the hydrochloride salt crystallized out. Next, 4.45 g. (0.033 mole) of sulfuryl chloride (freshly distilled) in 25 ml. of glacial acetic acid was added, with stirring, over a 30 minute period, dropwise. The temperature was 2627 C. throughout the addition. After 1 hour stirring, 250 ml. of dry ether was added slowly and crystallization began. After 15 min. the product was filtered off, washed with dry ether and air dried. The 7 g. obtained was dissolved in ml. of l N HCL, filtered, and the' pH adjusted, with cooling to 5 with conc. NH OH. The resulting crystalline product was filtered off after 5 min. standing, washed with two 20 ml. portions of water and 5x with acetone. The vacuum dried material weighed 4.6 g.; dec. pt. 217 C. (sharp). The NMR and IR spectra were consistent with the desired structure. [a] l 37.l (C 1 percent,

chloride 1N HCL) Anal. Calcd, for C H ClNO C, 47.76; H, Cl, 17.66. Found: C, 47. l6; H, 3.92; Cl, 17.96.

(1 l -2-( p-Methoxyphenyl )-glycine To a stirred solution of 19.6 g. (0.4 mole) of NaCN in ml. of H 0 was added 23.6 g. (0.450 mole) of NH Cl and 20 ml. of cone. NH OH followed by 54.5 g. (0.4 mole) of anisaldehyde in 160 ml. of methanol and the temperature maintained at 37 C. for 2 hours. The methanol was then removed in vacuo and the remaining mixture extracted with two ml. portions of methyl isobutyl ketone MlBK and combined. The combined MIBK extracts were washed once with 30 ml. of H 0 and then 240 ml. of 6 N HCl added with good mixing and the MljBK was removed in vacuo. The resulting slurry was heated at reflux (now in solution) for 2 hours. One hundred ml. of H 0 was added to the hot .filtrates (hot) were stirred and treated with cone.

NH OH until pH 5-6 was obtained (pH paper). The slurry was then cooled to 5 C. and after 1 hour the crystals were filtered off and washed with two 100 ml. portions of water. The damp cake was then slurried in 250 ml. of water and 50 percent NaOH added slowly until the product dissolved. Two 300 ml. ether extracts were then taken and discarded. The pH was then adjusted to 5.5 with 6 N HCl with cooling. After 1 hour the product was filtered off, washed with 3 X 100 ml. H and air dried. Yield 40 g.; dec. 244 C. with sublimation at 230 C.

d l -2-( p-Methoxyphenyl )-N-( chloroacetyl) glycine To a stirred suspension of 36 g. (0.2 mole) of d1-2- (p-methoxyphenyl)-glycine in 500 ml. of H 0 was added 8 g. (0.2 mole of NaOH pellets and when a clear solution was obtained the solution was cooled to C. and with vigorous stirring 68.2 g. (0.4 mole) of chloroacetic anhydride (warm) was added all at once. Then a solution of 16 g. (0.4 mole) of NaOH in 100 ml. of H 0 was added over a 10 to minute period. More percent NaOH was added as needed to keep the pH at about 9 for a 1.5 hour period. Next, the pH was ad justed to 2 with 40 percent H PO The product crystallized immediately and was filtered off, washed with water and recrystallized from ethanol-water to give 38 g. of product melting at 182-183 C.

Anal. Calcd. for C H ClNO z C, 51.21; H, 4.69. Found: C, 51.49; H, 4.90

D-(-)-2-(p-Methoxyphenyl)-N-chloroacetylglycine and L-(+)-2-(pMethoxyphenyl)-glycine To 800 ml. of H 0 stirred at 37 C. was added 38 g. (0.148 mole) of d1-2-(p-methoxyphenyl)-N- chloroacetylglycine and NH OH added dropwise until pH 7.8 was obtained. To the resulting solution was added 2 g. of hog kidney acylase (Sigma Chemical Company) and stirring continued at 37 C. (internal) for 21 hours. The solids containing crude L-(+)-2-(pmethoxyphenyl)-glycine were then filtered off and washed with 2 X 100 ml. H 0 and the pH of the combined filtrates adjusted to 4-5 with glacial acetic acid. This solution was heated on the steam bath for min. with 5 g. of decolorizing carbon and then filtered. The carbon cake was washed with 50 ml. of warm water and the combined filtrates cooled and acidified to pH 2 with 40 percent H PO After one hour cooling at 0 C. the crystalline product was filtered off and washed with cold water (3x) and air dried. The yield was 16 g. D-(- )-2-(p-methoxyphenyl)-N-chloroacetylglycine and when a second run using 5x the above amounts were used a yield of 83 g. (87% yield) was obtained. M. p. 170 171 C.; [01],} C. -193 (C 1 percent, ethanol) Anal. Calcd. for C H ClNO C, 51.21; H, 4.69. Found: C, 51.50; H, 4.99.

When the solids containing crude L-(+)-2-(pmethoxy-phenyD-glycin are treated with hot 3 N HCl (200 ml.) and carbon followed by filtration and pH adjustment to 5.5 there is obtained 6 g. (first run) of pure D-(-)-2-(p-Methoxyphenyl)-glycine The 16 g. of D-(-)-2-(p-methoxyphenyl)-N- chloroacetylglycine was refluxed 1.5 hours in 170 ml. of 2 N HCL. The resulting clear solution was filtered and cooled at 5 C. and the pH adjusted to 5.5 with NH OH. The product was then filtered off after cooling 30 min. and washed with 3 25 ml. of cold water. The dried material D-(-)-2-(p-methoxyphenyl) glycine weighed 9.5 g. A second run gave 54 g.

[111 1. +-149.9 (C =1%, l N HCL) (first run) [c11 148.1 (C= 1%, 1 N HCL) (second run) Anal. Calcd. for C H NO C, 59.67; H, 6.13; N, 7.74. Found: C, 59.38; H, 6.16; N, 8.00.

D-(-)-2-(p-Hydroxyphenyl)-glycine A mixture of 1.81 g. (0.01 mole) of D-(-)-2-(pmethoxyphenyl)glycine ([cd C. -149.9 C=1%, l N HCl) and 10 ml. of 48% HBr was heated at gentle reflux for 2 hours. The resulting solution was concentrated at reduced pressure at 30 C. to a wet solid. A minimum amount of water (20 C.) was added to dissolve the HBr salt and with cooling NH OH was added to pH 5. The resulting thick gel which ppt. was warmed to 50 C. and when solution was nearly obtained a different crystalline form began to ppt. Upon cooling 30 min. at 0-5 C. there was obtained 990 mg. of cold water washed (3 X 1 ml.) and air dried material, D-(-)- 2-(p-hydroxyphenyl)-glycine. [01],? C. 161.2 (C =l%, 1 N HCl) dec. pt. 223 C. A second run using 20 X the above amounts gave 24.5 g. of material. [a],, C. 153 (C=1% 1 NHCl) Anal. calcd. for C H NO z C, 57.49; H, 5.43; N, 8.39. Found: C, 57.41; H, 5.67; N, 8.39.

D-(-)-2-(3,5-dichloro-4-hydroxyphenyl)-glycine To a stirred suspension of 5.01 g. (0.03 mole) of D-(- )-2-(4-hydroxyphenyl)glycine in 100 ml. of glacial acetic acid was bubbled in HCl gas at a vigorous rate for about 5 minutes. At first a clear solution resulted and then the hydrochloride salt crystallized out. Next, 9.0 g. (0.067 mole) of sulfuryl chloride (freshly distilled) in 25 ml. of glacial acetic acid was added, with stirring, over a 30 minute period, dropwise. The temperature was 2627 C. throughout the addition. After the sulfuryl chloride addition, the slurry was heated to C. for 30 minutes and then stirred at ambient temperature for 2 hours. Then 250 ml. of dry ether was added slowly and crystallization began. After 15 min. the product was filtered off, washed with dry ether and air dried. The 7 g. obtained was dissolved in ml. of 1 N HCl, filtered, and the pH adjusted, with cooling to 5 with conc. NH OH. The resulting crystalline product was filtered off after 5 min. standing, washed with two 20 ml. portions of water and 5X with acetone. The vacuum dried material weighed 4.5 g.; dec. pt. 210 C. (sharp). The NMR and IR spectra were consistent with the desired structure. ]a] 126.3 (C=1%,1N HCl) Anal. Calcd. for C H Cl NO C, 40.78; H, 2.99; CI, 30.04. Found: C, 41.85; H, 3.22; Cl, 27.80.

Resolution of DL-a-amino-3-methoxyphenylacetic acid DL-a-Amino-3-methoxyphenylacetic acid [A. H.

Neims, 'D. C. DeLuca, L. Hellerman, Biochemistry, 5-

(l 203 1966)] was resolved with d-lO-camphorsulfonic acid in water.

DL-a-Amine-3-methoxyphenylacetic acid (33.1 g., 0.182 mole) was added to a solution of 46.4 g. (0.2 mole) of d-lO-camphorsulfonic acid in ml. of water at 50 to 60. The solution was filtered and stored in the cold for 20 hours. The precipitated amino acid d-- camphorsulfonate salt was collected by filtration. The salt was repeatedly recrystallized from water until a sample of the amino acid regenerated from it showed no further change in optical rotation. Thus, after three recrystallizations from water, there was obtained 3.7 g. of the d-IO-camphorsulfonate salt of D-a-amino-3- methoxyphenylacetic acid; m.p. 184-185 dec. The salt (1.4 g.) was dissolved in about 10 ml. of water by warming. The solution was adjusted to pH 5-6 with concentrated ammonium hydroxide. The product was allowed to crystallize first at room temperature and then in an ice bath giving, after filtration and drying in vacuo over phosphorus pentoxide, 0.36 g. of Daamino-3methoxyphenylacetic acid; m.p. l78-181 dec., [a] =129.0 (C =05, 1 N HCl). A portion of the amino acid was recrystallized from water and dried in vacuo over phosphorus pentoxide; m.p. 180182 dec., [a],, =136(C=0.08, 1 N HCl).

Anal. Calcd. for C H NO .l/3 H O: C, 57.74; H, 6.28; N, 7.48. Found: C, 57.70; 57.76; H, 6.23; 6.18; N, 7.21.

D-a-Amino-3-hydroxyphenylacetic acid hydrobromide monohydrate D-a-Amino-3-methoxyphenylacetic acid (2.9 g., 0.016 mole) and 16 ml. of 48 percent hydrobromic acid were refluxed for 2 hours. The volatile materials were removed at reduced pressure. Water (about ml.) was added to the residue and this removed at reduced pressure. This was repeated once. The residue was dried in vacuo to remove all water. The dried residue was recrystallized by dissolving in 2-propanol and adding Skellysolve B to the cloud point. After drying there was obtained 3.0 g. of D-a-amino-S-hydroxyphenylacetic acid hydrobromide monohydrate; m.p. l56l62 dec., [a],, =-62 (C =0. 1, water). The infrared and nuclear magnetic resonance spectra were consistent with the desired product.

Anal. Calcd. for C H NOgHBr- H O: C, 36.10; H, 4.55; N, 5.26. Found: C, 37.03; H, 5.12; N, 5.34.

2. D-a-Acetamido-3nitrophenylacetic acid A stirred suspension of 49.8 g. (0.254 mole) of D-aamino-3nitrophenyl-acetic acid [P. Fries, K. Kjaer, Acta Chimica Scand., ]7, 2391 (1963)] in 500 ml. of water was cooled in an ice bath and a solution of 8.36 g.

(0.209 mole) of NaOH in 40 ml. of water was addedcausing most of the solid to dissolve. There was immediately added 42.7 g. (0.418 mole) of acetic anhydride followed by the addition as needed of a solution of 25.1 g. (0.627 mole) of sodium hydroxide to maintain the pH value at about 7. The reaction mixture was stirred in the ice bath for an additional 15 minutes, filtered, and adjusted to pH 1.8 with concentrated hydrochloric acid. The crystalline product was collected by filtration and washed with water; yield 25 g., m.p. 172l74 dec. The product was twice recrystallized from 1:1 95 percent ethanol-water giving, after drying in vacuo over phosphorus pentoxide, l 1.8 g. of D-a-acetamido-3-nitrophenylacetic acid, m.p. 183-l 8 5; [a] "=-l 79.4 (C =0.5, 95 percent ethanol). The infrared and nuclear magnetic resonance spectra were consistent with the desired compound.

Anal. Calcd. for C H N O z C, 50.42; H, 4.23; N, 11.76. Found: C, 50.56; H, 4.20; N, 11.73.

D-a-Acetamide-3-aminophenylacetic acid. A solukeep the temperature under 40. The catalyst was removed by filtration. Evaporation of the filtrate gave a crystalline product. Two recrystallizations from 1- propanol gave 3.4 g. of D-a-acetamido-3-aminophenylacetic acid, m.p. 200-201 dec.; [a] l74.4 (C =0.5, water).

Anal. Calcd. for 0 11 81 0 C, 57.71; H, 5.81; N, 13.46. Found: C, 57.78; H, 5.97; N, 13.35.

D-a-Amino-3hydroxyphenylacetic acid A solution of 2.1 g. (0.01 mole) of D-a-acetamido-3- aminophenylacetic acid in 35 ml. of trifluoroacetic acid was cooled to 5 and 0.69 g. 0.01 mole) of solid sodium nitrite added. After stirring for 20 minutes at 5 acetic acid (5 ml.) was added. The mixture was stirred at 45 to 50 for 1% hours and then heated on the steam bath for one-half hour. The cold reaction mixture was poured onto 30 g. of crushed ice. The volatile materials were distilled at reduced pressure leaving as residue a slightly brown viscous oil. The residue was combined with 30 ml. of 2 N hydrochloric acid and refluxed for 1 19 hours. The volatile materials were removed under reduced pressure. Water was added to the residue and this removed under reduced pressure causing the hydrochloride salt of the product to crystallize. The residue was dissolved in a minimum amount of water, adjusted to pH 4.5 with 20 percent sodium hydroxide, filtered, and stored in the cold giving 0.43 g. of crystalline D-oz-amino-3-hydroxyphenylacetic acid, m.p. 204206 dec. The filtrate was stripped to dryness and a small amount of water added to the crystalline residue giving a second crop (0.46 g.) of the amino acid.

The filtrate from the second crop plus 3 m1. of concentrated hydrochloric acid were concentrated to dryness. The residue was dissolved in a small amount of water by warming, cooling gave crystalline D-a-amino- 3-hydroxyphenylacetic acid hydrochloride monohydrate; yield 0.5 g., m.p. l53 dec., [04],, 9l.2 (C =0.5, water). The infrared and nuclear magnetic resonance spectra were consistent with the desired product.

Anal.- Calcd. for C H N0 -HCl-H O: C, 43.35; H, 5.46; N, 6.32. Found: C, 42.7; H, 5.6; N, 6.17; residue, 1.45. Values corrected for 1.45 percent residue: C, 43.3; H, 5.7; N, 6.26.

The two crops of D-a-amino-3hydroxyphenylacetic acid were combined, suspended in a small amount of water, 2 ml. of 48 percent hydrobromic acid added and the filtered solution evaporated to dryness. The residue was twice recrystallized from water giving 150 ml. of D- a-amino3-hydroxyphenylacetic acid hydrobromide monohydrate; m.p. 172-175 dec., [a],, =74 (C 0.1, water). The infrared and nuclear magnetic resonance spectra were consistent with the assigned structure.

Anal. Calcd. for C H NO -HBr-H O: C, 36.10; H, 4.55; N, 5.26. Found: C, 36.20; H, 4.62; N, 5.32.

3. D-a-Amino-3-hydroxyphenylacetic acid 3. A solution of 38.4 g. (0.1845 mole) of D-aacetamido-3-aminophenylacetic acid in 600 ml. of trifluoroacetic acid prepared at to was cooled to 5 and 13 g. (0.1845 mole) of 98 percent sodium nitrite added in portions during a lO-minute period with stirring at -5. After stirring for an additional minutes 90 ml. of acetic acid was added at -5 to 0. The mixture was heated at 45 to 50 for 1% hours (gas evolution), refluxed for one-half hour, cooled, and poured onto 500 g. of ice flakes. The volatile materials were removed at reduced pressure. The residue was refluxed with 400 ml. of 2 N hydrochloric acid for 1 hour. Concentration to a small volume gave the crystalline hydrochloride salt. The dried product (27 g.) was recrystallized from wet acetic acid (150 ml. acetic acid plus 7 ml. of water) giving 21 g. of D-a-amino-3- hydroxyphenylacetic acid hydrochloride monohydrate; m.p. 149-152 dec., [01], =103.0(C= 0.5, water).

D-a-amino-4-acetamidophenylacetic acid D-a-acetamido-4-aminophenylacetic acid (39.2 g., 0.188 mole) in 400 ml. of 2 N hydrochloric acid was refluxed for 2 hours. The mixture was concentrated to dryness at reduced pressure. Water was added and the solution again concentrated to dryness. This was repeated once. The crystalline residue was slurried with 2-propanol, filtered, and washed additionally with 2- propanol giving, after air drying, 47 g. of the hydrochloride of D-a-amino-4-arninophenylacetic acid.

Ten g. of the hydrochloride in 40 ml. of water was adjusted to pH 4.8 with 20 percent sodium hydroxide. Crystalline D-a-amino-4-aminophenylacetic acid separated. To the solution obtained by adding 160 ml. additional of water was added 10 ml. of thioacetic acid. The mixture was stirred for 17 hours at 24 under a nitrogen atmosphere. The reaction mixture, containing a quantity of crystalline product, was concentrated to one-half of its initial volume giving 4.5 g. of product. The crude product was suspended in water, the suspension adjusted to pH 4.6 with 20 percent NaOH, heated to 95, carbon treated, and the product allowed to crystallize in the cold overnight. The resulting gelatinous mass was broken up by warming. The solid was removed by filtration; wt. 0.2 g., m.p. 203-206 dec. The filtrate was diluted withan equal volume of 95 percent ethanol giving 1.4 g. of D-a -amino-4- acetamidophenylacetic acid; m.p. 2l4-215 dec., [a] =133.4(C=0.5,1NHC1).

Anal. Calcd. for C H N o z C, 57.71; H, 5.814; N, 13.46. Found: C, 56.80, 56.72; H, 5.84, 5.89; N, 13.62; H O, 1,32. Found values corrected for 1.32 percent water: C, 57.52; H, 5.71; N, 13.80.

D-a-amino-3-aminophenylacetic acid A solution of 9.8 g. (0.05 mole) of D-a-amino- 3nitrophenylacetic acid [1. Friis and A. Kjaer, Acta Chimica Scand. 17, 2391 (1963); British Patent Specification, 1,033,257] in 200 ml. of water was prepared by adjusting the mixture to pH 9.3 with concentrated ammonium hydroxide. The solution was hydrogenated for 1 hour in the presence of 0.4 g. of 5 percent palladium on carbon on a Paar hydrogenation apparatus at an initial pressure of 50 psi. The vessel was cooled as needed to keep the temperature from going above After 1 hour an additional 0.4 g. of catalyst was added and hydrogenation continued for 1 hour longer. Three additional runs were made hydrogenating a total of 39.4 g. of nitro compound. Addition of the second amount of catalyst was omitted in the additional runs and a hydrogenation time of about 1 hour was used. Each run was filtered to remove catalyst, the filtrates pooled and concentrated to a small volume until crystallization of the product started. The concentrate was diluted with about five volumes of percent ethanol, the mixture stored overnight in the coldand the product filtered and washed further by slurrying with 95 percent ethanol. After drying in a vacuum oven for 3 hours at 40 and then in vacuo over phosphorus pentoxide for 64 hours there was obtained 25.7 g. of D- a-amino-3-aminophenylacetic acid; m.p. 188191, [a 1 =-139.0 (C=1 in HCl).

The preparation of this compound has been described by P. Friis and A. Kjaer, Acta Chimica Scand. 17,2391 (1963).

D-a-amino-3-acetamidophenylacetic acid A mixture of 5 g. (0.0301 mole) of D-a-amino-3- aminophenylacetic acid and 5 ml. of thioacetic acid in ml. of water was stirred for 16 hours under a nitrogen atmosphere. The mixture was heated on a steam bath for one-half hour and then concentrated at reduced pressure to a small volume. On cooling the concentrate the product started to crystallize. The concentrate was diluted with 95 percent ethanol and, after chilling in an ice bath, the product was filtered and washed with 95 percent ethanol; wt. 1.8 g. The filtrate was further diluted with 95 percent ethanol giving an additional 2.3 g. of product. The two crops of product were combined, dissolved in a small amount of water by warming, the solution concentrated slightly and diluted with a large volume of 95 percent ethanol. The initial crop of solid was removed by filtration and the filtrate stored in the cold for 16 hours giving,after dry ing at 65 for 3 hours in vacuo over phosphorus pentoxide, 0.90 g. of product, m.p. 185-l87 dec. The product was twice recrystallized from 1:1 95 percent ethanol-water; wt. 0.36 g., m.p. 186187 dec. [11],, (C=0.5, 1 N HCl).

Anal. Calcd. for C fl N O z C, 57.7; H, 5.81; N, 13.5. Found: C, 47.29; H, 6.79; H, 11.21;H O, 18.3. Found values corrected for 18.3 percent water: C, 57.9; H, 5.83;N, 13.7.

DL-a-Amino-3-chlorophenylacetic acid A solution of 250 g. of m-chlorobenzaldehyde in 1.5 l. of 95 percent ethanol was added in one-portion to a stirred solution of 123 g. of sodium cyanide, 515 g. of ammonium carbonate and 1.5 l. of water. The mixture was stirred at 50 for 120 hours. The cooled reaction mixture was acidified to pH 2 with concentrated hydrochloric acid and stirred 1 hour. The hydantoin was collected by filtration, washed with cold water, and sucked dry on the filter.

A mixture of the crude hydantoin obtained from two runs and 4 l. of 10 percent sodium hydroxide was refluxed for 18 hours. The solution was carbon treated and neutralized to pH 7 with acetic acid. The solid was collected by filtration, washed with water, and dried on the filter. A suspension of the product in 4 1. of water was acidified to pH 2 with concentrated hydrochloric 

2. A compound of the formula
 3. A compound as defined in claim 2 wherein A is acetoxy.
 4. A compound as defined in claim 2 wherein A is hydrogen.
 5. A compound as defined in claim 2 wherein A is pyridinium.
 6. A compound as defined in claim 2 wherein A is acetoxy and Z is phenyl, 2-thienyl, 3-thienyl, 2-furyl or 5-nitro-2-furyl.
 7. A compound as defined in claim 2 wherein A is hydrogen and Z is phenyl, 2-thienyl, 3-thienyl, 2-furyl or 5-nitro-2-furyl.
 8. A compound as defined in claim 2 wherein A is pyridinium and Z is phenyl, 2-thienyl, 3-thienyl, 2-furyl or 5-nitro-2-furyl.
 9. A compound as defined in claim 6 in the D configuration.
 10. A compound as defined in claim 7 in the D configuration.
 11. A compound as defined in claim 8 in the D configuration.
 12. The acid as defined in claim 9 of the formula
 13. The acid as defined in claim 10 of the formula
 14. The acid as defined in claim 9 of the formula
 15. The compound as defined in claim 11 of the formula
 16. The acid as defined in claim 9 of the formula
 17. The compound as defined in claim 11 of the formula
 18. The acid as defined in claim 9 of the formula
 19. The compound as defined in claim 11 of the formula 